Technical field
[0001] The present invention relates to a halogen-free resin composition, and a prepreg
and a laminate which are prepared by using the same and have advantages of low dielectric
constant, low dielectric loss factor, low water absorption, high dimensional stability,
high thermal resistance and good flame retardancy, processability and chemical resistance,
etc.
Background art
[0002] Traditional laminates used for printed circuit mainly utilize brominated flame retardants
to achieve flame retardancy, in particular utilize tetrabromobisphenol-A epoxy resin
which has good flame retardancy but can produce hydrogen bromide gas when burning.
In addition, in recent years, carcinogens such as dioxins, dibenzofurans and others
have been detected in the combustion products of wastes of electrical and electronic
equipments containing halogen such as bromine, chlorine and the like, and thus the
use of brominated epoxy resin is limited. On July 1, 2006, two environmental protection
directives of the European Union "Directive on the waste electrical and electronic
equipment" and "Directive on the restriction of the use of certain hazardous substances
in electrical and electronic equipment" were officially implemented. The development
of halogen-free flame retardant copper-clad laminates has become a hot topic in the
related industry field, and each copper-clad laminate manufacturer has launched their
own halogen-free flame retardant copper-clad laminate in succession.
[0003] With the development of high-speed and multi-functionalization of information processing
of electronic products, the frequency applied is increasing. In addition to a higher
demand for thermal resistance of laminate materials, there is also a demand that the
dielectric constant and the dielectric loss value become lower and lower, and thus
reducing Dk/Df has become a hot spot pursued by the practitioners in substrate industry.
Traditional FR-4 materials mainly utilize dicyandiamide as a curing agent. This curing
agent has reactive tertiary amine and has good processing operability, but since its
C-N bond is weak and easy to crack at a high temperature, resulting in a lower thermal
decomposition temperature for the cured product, it cannot meet the demand for thermal
resistance during the lead-free manufacturing process. In this background, with the
wide implementation of the lead-free technology in 2006, phenolic resin began to be
used as an epoxy curing agent in the industry. Phenolic resin has benzene ring structures
with high density, and thus the thermal resistance of a cured system of phenolic resin
and epoxy resin is excellent, but the dielectric properties of the cured product have
a trend of being worsen.
[0004] CN 101914265A discloses a halogen-free phosphorus-containing flame retardant high-frequency epoxy
resin composition. In the resin composition of the invention, conventional brominated
difunctional epoxy resin is substituted by multifunctional epoxy resin; conventional
dicyandiamide is substituted by linear phenolic resin serving as a curing agent. The
epoxy resin composition consists of benzoxazine epoxy resin, tetraphenol ethane epoxy
resin, DOPO modified phenolic resin, alkyl modified phenolic resin, imidazole accelerating
agent, inorganic filler, inorganic auxiliary flame retardant filler and the like.
The bonding sheet and the copper-clad plate, which are prepared from the epoxy resin
composition and are used for a printed circuit board, have environmentally-friendly
flame retardancy and excellent dielectric performance. But the bonding sheet and the
copper-clad laminate have a water absorption being up to 0.3%-0.4%, and thus can absorb
moisture easily resulting in delamination in the subsequent process for preparing
PCB, and the dielectric properties thereof are common, therefore it is difficult to
meet the requirements for development of high frequency in electronic signal transmission
and high-speed in information processing in the industry of printed circuit copper
clad laminate.
Contents of the invention
[0005] In view of the problems existing in the prior arts, the purposes of the present invention
lie in providing a novel halogen-free low dielectric resin composition, and a prepreg
and a laminate prepared by using the same. The laminate used for printed circuit prepared
by using the resin composition has low dielectric constant, low dielectric loss factor,
low water absorption, high dimensional stability, high thermal resistance and good
flame retardancy, processability and chemical resistance, etc.
[0006] In order to achieve the above purposes, the present inventors carried out repeated
and in-depth researches and found that: a composition obtained by appropriately mixing
alkyl phenol epoxy resin with benzoxazine resin, alkyl phenol novolac curing agent,
phosphorus-containing flame retardant and other optional components can achieve the
purposes.
[0007] A halogen-free resin composition comprising the following components:
- (A) alkyl phenol epoxy resin;
- (B) benzoxazine resin;
- (C) alkyl phenol novolac curing agent;
- (D) phosphorus-containing flame retardant.
[0008] The alkyl phenol epoxy resin used in the present invention has many alkyl branched
chains in its molecular structure, making the composition have excellent dielectric
properties while it has higher glass transition temperature, low water absorption,
good heat resistance. Mixing benzoxazine resin into the composition can further reduce
dielectric constant, dielectric loss value and water absorption of the cured product.
With alkyl phenol novolac being used as a curing agent, the advantages that the molecular
structure thereof has many alkyls and thus the dielectric properties are excellent
and the water absorption is low are fully played.
[0009] The present invention obtained the above halogen-free low dielectric resin composition
by utilizing the mutual cooperation and synergistic interaction of the above three
necessary components and by adding phosphorus-containing flame retardant. The prepreg
and the laminate used for printed circuit prepared by using the halogen-free low dielectric
resin composition have low dielectric constant, low dielectric loss factor, low water
absorption, high dimensional stability, high thermal resistance and good flame retardancy,
processability and chemical resistance.
[0010] The component (A), i.e. the alkyl phenol epoxy resin, can improve the electrical
property, moisture resistance, heat resistance and mechanical property required by
the cured resin and the laminate prepared by using the same. Based on 100 parts by
weight of the organic solid matters, the addition amount of the alkyl phenol epoxy
resin is 10-50 parts by weight, for example 13 parts by weight, 16 parts by weight,
19 parts by weight, 22 parts by weight, 25 parts by weight, 28 parts by weight, 31
parts by weight, 34 parts by weight, 37 parts by weight, 40 parts by weight, 43 parts
by weight, 46 parts by weight or 49 parts by weight, preferably 20-50 parts by weight.
[0011] In the present invention, the alkyl phenol epoxy resin having the above addition
amount can not only obviously improve the dielectric properties of the cured products
but also keep higher adhesion force.
[0012] Preferably, the alkyl phenol epoxy resin has the following structure:

wherein, R
1 and R
2 are independently substituted or unsubstituted straight alkyl or branched alkyl having
a carbon atom number of 4-8, preferably n-butyl or n-octyl; n is an integer between
2-20, for example 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18 or 19.
[0013] In the present invention, n-butyl or n-octyl has a regular structure, and thus the
dielectric properties and heat resistance thereof are good.
[0014] Preferably, based on 100 parts by weight of the organic solid matters, the addition
amount of the benzoxazine resin is 10-70 parts by weight, for example 13 parts by
weight, 16 parts by weight, 19 parts by weight, 22 parts by weight, 25 parts by weight,
28 parts by weight, 31 parts by weight, 34 parts by weight, 37 parts by weight, 40
parts by weight, 43 parts by weight, 46 parts by weight, 49 parts by weight, 52 parts
by weight, 55 parts by weight, 58 parts by weight, 61 parts by weight, 64 parts by
weight, 67 parts by weight or 69 parts by weight.
[0015] In the present invention, benzoxazine resin having the above addition amount can
improve the heat resistance and the rigidity of the cured products and can reduce
water absorption.
[0016] Preferably, the benzoxazine resin is any one of bisphenol-A benzoxazine resin, bisphenol-F
benzoxazine resin, MDA (4,4'-diaminodiphenylmethan) benzoxazine resin, phenolphthalein
benzoxazine resin or dicyclopentadiene benzoxazine resin, or a mixture of at least
two of them. Said mixture is for example a mixture of bisphenol-A benzoxazine resin
and bisphenol-F benzoxazine resin, a mixture of MDA benzoxazine resin and phenolphthalein
benzoxazine resin, a mixture of dicyclopentadiene benzoxazine resin and bisphenol-A
benzoxazine resin, a mixture of bisphenol-F benzoxazine resin, MDA benzoxazine resin,
phenolphthalein benzoxazine resin and dicyclopentadiene benzoxazine resin.
[0017] Preferably, based on 100 parts by weight of the organic solid matters, the addition
amount of the alkyl phenol novolac curing agent is 5-25 parts by weight, for example
6 parts by weight, 8 parts by weight, 10 parts by weight, 12 parts by weight, 14 parts
by weight, 16 parts by weight, 18 parts by weight, 20 parts by weight, 22 parts by
weight or 24 parts by weight.
[0018] In the present invention, alkyl phenol novolac curing agent having the above addition
amount can improve dielectric properties of the cured products and also can keep higher
adhesion force.
[0019] Preferably, the alkyl phenol novolac curing agent has the following structure:

wherein, R
3, R
4 and R
5 are independently substituted or unsubstituted straight alkyl or branched alkyl having
a carbon atom number of 4-8, preferably n-butyl or n-octyl; n
1 is an integer between 2-20, for example 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14,
15, 16, 17, 18 or 19.
[0020] The addition of phosphorus-containing flame retardant makes the resin composition
have flame retardant property and meet the requirements of UL 94V-0. Meanwhile, benzoxazine
resin has a synergistic flame retardant effect with phosphorus-containing flame retardant,
reducing the phosphorus content of the cured product required to achieve UL 94V-0
for flame retardancy, further reducing the water absorption. Preferably, based on
100 parts by weight of the total addition amount of component (A), component (B) and
component (C), the addition amount of the phosphorus-containing flame retardant is
550 parts by weight, for example 7 parts by weight, 9 parts by weight, 11 parts by
weight, 13 parts by weight, 16 parts by weight, 19 parts by weight, 22 parts by weight,
25 parts by weight, 28 parts by weight, 31 parts by weight, 34 parts by weight, 37
parts by weight, 40 parts by weight, 43 parts by weight, 46 parts by weight or 49
parts by weight.
[0021] Preferably, the phosphorus-containing flame retardant is any one of tri(2,6-dimethylphenyl)phosphine,
10-(2,5-dihydroxyphenyl)-9,10-dihydro-9-oxa-10-pho sphaphenanthrene-10-oxide, 2,6-bis(2,6-dimethylphenyl)
phosphinobenzene or 10-phenyl-9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide,
phenoxy phosphazene compound, phosphate or polyphosphate, or a mixture of at least
two of them.
[0022] Preferably, the halogen-free resin composition also comprises a curing accelerator,
which makes the resin cure and accelerate the curing rate of the resin. Based on 100
parts by weight of the total addition amount of component (A), component (B), component
(C) and component (D), the addition amount of the curing accelerator is 0.051 parts
by weight, for example 0.08 parts by weight, 0.1 parts by weight, 0.15 parts by weight,
0.2 parts by weight, 0.25 parts by weight, 0.3 parts by weight, 0.35 parts by weight,
0.4 parts by weight, 0.45 parts by weight, 0.5 parts by weight, 0.55 parts by weight,
0.6 parts by weight, 0.65 parts by weight, 0.7 parts by weight, 0.75 parts by weight,
0.8 parts by weight, 0.85 parts by weight, 0.9 parts by weight or 0.95 parts by weight.
[0023] Preferably, the curing accelerator is any one selected from the group consisting
of imidazole and/or pyridine curing accelerators, or a mixture of at least two of
them; preferably any one selected from the group consisting of 2-methyl imidazole,
2-ethyl-4-methyl imidazole, 2-phenyl imidazole, 2-undecyl imidazole, triethylamine,
benzyl dimethylamine or dimethylamino pyridine, or a mixture of at least two of them.
[0024] Preferably, the halogen-free resin composition also comprises a filler. The filler
is organic or/and inorganic filler, and mainly used to adjust some physical properties
of the composition, for example to reduce thermal expansion coefficient (CTE), water
absorption, and to improve thermal conductivity.
[0025] Preferably, based on 100 parts by weight of the total addition amount of component
(A), component (B), component (C) and component (D), the addition amount of the filler
is 0-100 parts by weight excluding 0, preferably 0-50 parts by weight excluding 0.
The addition amount of the filler is for example 0.5 parts by weight, 1 parts by weight,
5 parts by weight, 10 parts by weight, 15 parts by weight, 20 parts by weight, 25
parts by weight, 30 parts by weight, 35 parts by weight, 40 parts by weight, 45 parts
by weight, 50 parts by weight, 55 parts by weight, 60 parts by weight, 65 parts by
weight, 70 parts by weight, 75 parts by weight, 80 parts by weight, 85 parts by weight,
90 parts by weight or 95 parts by weight.
[0026] Preferably, the inorganic filler is any one selected from the group consisting of
fused silicon dioxide, crystalline silicon dioxide, spherical silicon dioxide, hollow
silicon dioxide, aluminum hydroxide, alumina, talcum powder, aluminum nitride, boron
nitride, silicon carbide, barium sulfate, barium titanate, strontium titanate, calcium
carbonate, calcium silicate, mica or glass fiber powder, or a mixture of at least
two of them. Said mixture is for example a mixture of fused silicon dioxide and crystalline
silicon dioxide, a mixture of spherical silicon dioxide and hollow silicon dioxide,
a mixture of aluminum hydroxide and alumina, a mixture of talcum powder and aluminum
nitride, a mixture of boron nitride and silicon carbide, a mixture of barium sulfate
and barium titanate, a mixture of strontium titanate and calcium carbonate, a mixture
of calcium silicate, mica and glass fiber powder, a mixture of fused silicon dioxide,
crystalline silicon dioxide and spherical silicon dioxide, a mixture of hollow silicon
dioxide, aluminum hydroxide and alumina, a mixture of talcum powder, aluminum nitride
and boron nitride, a mixture of silicon carbide, barium sulfate and barium titanate,
a mixture of strontium titanate, calcium carbonate, calcium silicate, mica and glass
fiber powder.
[0027] Preferably, the organic filler is any one selected from the group consisting of polytetrafluorethylene
powder, polyphenylene sulfide or polyethersulfone powder, or mixture of at least two
of them. Said mixture is for example a mixture of polytetrafluorethylene powder and
polyphenylene sulfide, a mixture of polyethersulfone powder and polytetrafluorethylene
powder, a mixture of polyphenylene sulfide and polyethersulfone powder, a mixture
of polytetrafluorethylene powder, polyphenylene sulfide and polyethersulfone powder.
[0028] Preferably, the filler is silicon dioxide, and the median of the particle diameter
thereof is 1-15µm, preferably 1-10µm. The filler with a particle size falling into
this range has a good dispersion.
[0029] The term "comprise(s)/comprising" used in the present invention means that in addition
to the components described, other components which give the halogen-free resin composition
different characteristics can also be included. In addition, the term "comprise(s)/comprising"
used in the present invention may also be replaced by a closed description as "is
/being" or "consist(s) of/consisting of".
[0030] For example, the halogen-free resin composition can also comprise a variety of additives,
and as specific examples, antioxidant, heat stabilizer, antistatic agent, UV absorber,
pigment, coloring agent, or lubricant and others can be listed. These additives can
be used alone, and can also be used in the form of a mixture of two or more of them.
[0031] A conventional method for preparing the halogen-free resin composition of the present
invention is: firstly adding solid matters, and then adding a liquid solvent, stirring
until the solid matters are completely dissolved, then adding a liquid resin and a
curing accelerator, and continuing to stir until the mixture is homogeneous, and finally
adjusting the solid content of the solution to 65%-75% by using a solvent to obtain
a varnish.
[0032] The second purpose of the present invention is to provide a prepreg comprising a
reinforcing material and the halogen-free resin composition as mentioned above which
is attached on the reinforcing material after impregnation and drying.
[0033] Exemplary reinforcing materials are nonwoven fabrics and/or other fabrics, for example,
natural fibers, organic synthetic fibers and inorganic fibers.
[0034] The varnish is used to impregnate reinforcing materials for example fabrics such
as glass cloth and the like or organic fabrics. The impregnated reinforcing material
is dried in an oven at 155°C for 5-10 min to obtain a prepreg.
[0035] The third purpose of the present invention is to provide a laminate comprising at
least one sheet of the prepreg as mentioned above.
[0036] The fourth purpose of the present invention is to provide a metal-clad laminate comprising
at least one sheet of the prepreg as mentioned above and metal foils overlapped on
one or two sides of the superimposed prepreg, and it is made by heating, pressing
and molding.
[0037] The metal-clad laminate is obtained by the following steps: 10 sheets of prepregs
mentioned above and 2 sheets of metal foils each of which has a thickness of 1 ounce
(35 µm thick) are superimposed together, and are laminated through a hot press machine
and thus are pressed into metal-clad laminate. Said lamination should meet the following
requirements: 1. the temperature rising rate for the lamination is usually controlled
at 1.5-2.5°C/min when the temperature of the materials is 80-220°C; 2. the pressure
conducted for the lamination is a full pressure which is about 350 psi when the temperature
of the outer materials is 120-150°C; 3. when curing, the temperature of the materials
is controlled at 190°C and the temperature is kept for 90 min. The metal foil is a
copper foil, a nickel foil, an aluminum foil and a SUS foil, etc., and the material
of the metal foil is not limited.
[0038] Compared with the prior arts, the present invention has the following beneficial
effects:
- 1) The halogen-free low dielectric resin composition of the present invention uses
alkyl phenol epoxy resin as one component; said epoxy resin has excellent dielectric
properties in addition to advantages of high glass transition temperature, low water
absorption, good heat resistance and others; 2) Mixing benzoxazine resin into the
composition can further reduce dielectric constant, dielectric loss value and water
absorption of the cured product; in addition, benzoxazine resin and phosphorus-containing
flame retardant have a synergistic flame retardant effect, reducing the phosphorus
content of the cured product required to achieve UL 94V-0 for flame retardancy, further
reducing the water absorption; 3) The halogen-free low dielectric resin composition
of the present invention uses alkyl phenol novolac as a curing agent, and the advantages
that the molecular structure thereof has many alkyls and thus the dielectric properties
are excellent and the water absorption is low are fully played; 4) the prepreg and
the laminate used for printed circuit prepared by using the resin composition have
advantages of low dielectric constant, low dielectric loss factor, low water absorption,
high thermal resistance, high dimensional stability and good flame retardancy, processability
and chemical resistance.
Embodiments
[0039] Hereinafter, the technical solutions of the present application are further described
by the specific embodiments.
[0040] With respect to the laminate (10 sheets of prepregs) used for printed circuit prepared
above, the properties of glass transition temperature, dielectric constant, dielectric
loss factor, bending strength, water absorption, heat resistance, flame resistance
and others thereof are tested.
[0041] The embodiments of the present invention are described in detail as follows, but
the present invention is not limited to the range of embodiments. In the following,
the "parts" means "parts by weight", and the "%" means "% by weight", unless otherwise
noted.
(A) epoxy resin
(A-1) alkyl phenol epoxy resin
KES-7595 (trade name, KOLON, Korea)
(A-2) bisphenol-Anovolac epoxy resin
EPR627MEK80 (trade name, Hexion, US)
(B) benzoxazine resin
LZ 8290H62 (trade name, HUNTSMAN)
(C) curing agent
(C-1) alkyl phenol novolac curing agent
KPT-F1350E (trade name, KOLON, Korea)
(C-2) linear novolac curing agent
2812 (trade name, MOMENTIVE, Korea)
(D) phosphorus-containing flame retardant
DOW XZ92741 (trade name, DOW, US)
(E) 2-phenyl imidazole (Shikoku chemicals corporation, Japan)
(F) filler
spherical silica powder (the average particle size thereof is 1 to 10 µm, and the
purity thereof is more than 99%)
Table 1. Formulas and physical data for each Example and Comparative Example
|
Example 1 |
Example 2 |
Example 3 |
Example 4 |
Example 5 |
A-1 |
50 |
40 |
30 |
20 |
10 |
A-2 |
--- |
--- |
--- |
--- |
--- |
B |
10 |
25 |
40 |
55 |
70 |
C-41 |
25 |
20 |
15 |
10 |
5 |
C-2 |
--- |
--- |
--- |
--- |
--- |
D |
15 |
15 |
15 |
35 |
5 |
E |
appropriate amount |
appropriate amount |
appropriate amount |
appropriate amount |
appropriate amount |
F |
40 |
40 |
40 |
40 |
40 |
glass transition temperature(DSC)°C |
172 |
164 |
166 |
158 |
175 |
dielectric constant(1GHz) |
3.55 |
3.57 |
3.61 |
3.60 |
3.67 |
dielectric loss(1GHz) |
0.0088 |
0.0085 |
0.0092 |
0.0090 |
0.0098 |
bending strength (N/mm2) |
504 |
532 |
551 |
575 |
578 |
water absorption (%) |
0.08 |
0.07 |
0.06 |
0.06 |
0.06 |
dip soldering resistance 288°C, s |
>120 |
>120 |
>120 |
>120 |
>120 |
flame retardancy |
V-0 |
V-0 |
V-0 |
V-0 |
V-0 |
Table 2. Formulas and physical data for each Comparative Example
|
Comparative Example 1 |
Comparative Example 2 |
Comparative Example 3 |
A-1 |
60 |
--- |
30 |
A-2 |
--- |
40 |
--- |
B |
--- |
25 |
40 |
C-1 |
25 |
20 |
--- |
C-2 |
--- |
--- |
15 |
D |
15 |
15 |
15 |
E |
appropriate amount |
appropriate amount |
appropriate amount |
F |
40 |
40 |
40 |
glass transition temperature(DSC)°C |
175 |
158 |
160 |
dielectric constant(1GHz) |
3.58 |
3.91 |
3.89 |
dielectric loss(1GHz) |
0.0095 |
0.0121 |
0.0134 |
bending strength (N/mm2) |
425 |
512 |
521 |
water absorption(%) |
0.12 |
0.09 |
0.08 |
dip soldering resistance 288°C,s |
55 |
>120 |
>120 |
flame retardancy |
V-0 |
V-0 |
V-0 |
[0042] Test methods for the above characteristics are as follows:
- (a) Glass transition temperature (Tg)
Glass transition temperature is tested according to differential scanning calorimetry
(DSC) as described by IPC-TM-650 2.4.25.
- (b) Dielectric constant and dielectric loss factor
Dielectric constant and dielectric loss factor are tested at 1 GHz according to the
resonance method using a strip line, in accordance with IPC-TM-650 2.5.5.5.
- (c) Bending strength
Bending strength is tested according to IPC-TM-650 2.4.4 method, by applying the load
on a sample having specified size and shape at room temperature.
- (d) Water absorption
Water absorption is tested according to IPC-TM-650 2.6.2.1 method.
- (e) Dip soldering resistance
Dip soldering resistance is tested according to IPC-TM-650 2.4.13.1 by observing the
time of delamination and blister.
- (f) Flame retardancy
Flame retardancy is tested according to UL 94 vertical combustion method.
[0043] From the physical data in table 1 and table 2, it can be seen that in Comparative
Example 1 when alkyl phenol epoxy resin is cured with alkyl phenol novolac curing
agent, the dielectric properties thereof are better, but the water absorption is high
and the bending strength is low and the heat resistance is poor; in Comparative Example
2, bisphenol-A novolac epoxy resin is co-cured with benzoxazine resin and alkyl phenol
novolac curing agent, and in Comparative Example 3, alkyl phenol epoxy resin is co-cured
with benzoxazine resin and linear novolac resin, and the cured products have poor
dielectric properties, high dielectric constant and high dielectric loss when only
one of the alkyl phenol epoxy resin and the alkyl phenol novolac curing agent is present.
In Examples 1-5, when alkyl phenol epoxy resin is co-cured with benzoxazine resin
and alkyl phenol novolac curing agent, the obtained laminates have excellent dielectric
properties, water absorption, high bending strength and high heat resistance.
[0044] As can be known from this, only when alkyl phenol epoxy resin, benzoxazine resin
and alkyl phenol novolac curing agent are present at the same time, a laminate with
excellent comprehensive properties can be obtained due to the mutual synergistic effect
of the three components. Comparative Examples 1-3 do not utilize benzoxazine resin,
alkyl phenol epoxy resin and alkyl phenol novolac curing agent respectively, so the
comprehensive properties of obtained laminates in Comparative Examples 1-3 are obviously
worse than that of the laminates in the Examples 1-5.
[0045] Therefore, compared to conventional halogen-free laminates, the laminate used for
printed circuit of the present invention has more excellent dielectric properties,
moisture resistance and dimensional stability, and thus is suitable for high density
interconnector field. In addition, the present invention makes full use of the synergistic
characteristic of benzoxazine resin and phosphorus-containing flame retardant, and
the halogen content can achieve V-0 standard in flame retardancy experiment UL94 in
the range of JPCA halogen-free standard, and thus the laminate of the present invention
has environmental protection effect.
[0046] The above are only better examples of the present invention. Those skilled in the
art can make a variety of other corresponding changes and modifications, and the changes
and modifications all should fall into the scope of the claims of the present invention.
[0047] The applicant states that: the present application illustrates the detailed compositions
of the present invention by the above examples, but the present invention is not limited
to the detailed compositions, that is, it does not mean that the invention must be
conducted relying on the above detailed compositions. Those skilled in the art should
understand that any modification to the present invention, any equivalent replacement
of each raw material of the present invention and the addition of auxiliary ingredient,
the selection of specific embodiment and the like all fall into the protection scope
and the disclosure scope of the present invention.
1. A halogen-free resin composition,
characterized in that, it comprises the following components:
(A) alkyl phenol epoxy resin;
(B) benzoxazine resin;
(C) alkyl phenol novolac curing agent;
(D) phosphorus-containing flame retardant.
2. The halogen-free resin composition of claim 1, characterized in that, based on 100 parts by weight of the organic solid matters, the addition amount of
the alkyl phenol epoxy resin is 10-50 parts by weight, preferably 20-50 parts by weight.
3. The halogen-free resin composition of claim 1,
characterized in that, the alkyl phenol epoxy resin has the following structure:

wherein, R
1 and R
2 are independently substituted or unsubstituted straight alkyl or branched alkyl having
a carbon atom number of 4-8, preferably n-butyl or n-octyl; n is an integer between
2-20.
4. The halogen-free resin composition of claim 1 or 2, characterized in that, based on 100 parts by weight of the organic solid matters, the addition amount of
the benzoxazine resin is 10-70 parts by weight.
5. The halogen-free resin composition of claim 1 or 2, characterized in that, the benzoxazine resin is any one of bisphenol-A benzoxazine resin, bisphenol-F benzoxazine
resin, MDA benzoxazine resin, phenolphthalein benzoxazine resin or dicyclopentadiene
benzoxazine resin, or a mixture of at least two of them.
6. The halogen-free resin composition of claim 1 or 2, characterized in that, based on 100 parts by weight of the organic solid matters, the addition amount of
the alkyl phenol novolac curing agent is 5-25 parts by weight.
7. The halogen-free resin composition of claim 1 or 2,
characterized in that, the alkyl phenol novolac curing agent has the following structure:

wherein, R
3, R
4 and R
5 are independently substituted or unsubstituted straight alkyl or branched alkyl having
a carbon atom number of 4-8, preferably n-butyl or n-octyl; n
1 is an integer between 2-20.
8. The halogen-free resin composition of claim 1 or 2, characterized in that, based on 100 parts by weight of the total addition amount of component (A), component
(B) and component (C), the addition amount of the phosphorus-containing flame retardant
is 5-50 parts by weight.
9. The halogen-free resin composition of claim 1 or 2, characterized in that, the phosphorus-containing flame retardant is any one of tri(2,6-dimethylphenyl)phosphine,
10-(2,5-dihydroxyphenyl)-9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide, 2,6-bis(2,6-dimethylphenyl)
phosphinobenzene or 10-phenyl-9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide,
phenoxy phosphazene compound, phosphate or polyphosphate, or a mixture of at least
two of them.
10. The halogen-free resin composition of claim 1 or 2, characterized in that, the halogen-free resin composition also comprises a curing accelerator, and based
on 100 parts by weight of the total addition amount of component (A), component (B),
component (C) and component (D), the addition amount of the curing accelerator is
0.05-1 parts by weight.
11. The halogen-free resin composition of claim 10, characterized in that, the curing accelerator is any one selected from the group consisting of imidazole
or/and pyridine curing accelerators, or a mixture of at least two of them; preferably
any one selected from the group consisting of 2-methyl imidazole, 2-ethyl-4-methyl
imidazole, 2-phenyl imidazole, 2-undecyl imidazole, triethylamine, benzyl dimethylamine
or dimethylamino pyridine, or a mixture of at least two of them.
12. The halogen-free resin composition of claim 1 or 2, characterized in that, the halogen-free resin composition also comprises a filler, and the filler is organic
or/and inorganic filler.
13. The halogen-free resin composition of claim 12, characterized in that, based on 100 parts by weight of the total addition amount of component (A), component
(B), component (C) and component (D), the addition amount of the filler is 0-100 parts
by weight excluding 0, preferably 0-50 parts by weight excluding 0.
14. The halogen-free resin composition of claim 12, characterized in that, the inorganic filler is any one selected from the group consisting of fused silicon
dioxide, crystalline silicon dioxide, spherical silicon dioxide, hollow silicon dioxide,
aluminum hydroxide, alumina, talcum powder, aluminum nitride, boron nitride, silicon
carbide, barium sulfate, barium titanate, strontium titanate, calcium carbonate, calcium
silicate, mica or glass fiber powder, or mixture of at least two of them.
15. The halogen-free resin composition of claim 12, characterized in that, the organic filler is any one selected from the group consisting of polytetrafluorethylene
powder, polyphenylene sulfide or polyethersulfone powder, or a mixture of at least
two of them.
16. The halogen-free resin composition of claim 12, characterized in that, the filler is silicon dioxide, and the median of the particle diameter thereof is
1-15µm, preferably 1-10µm.
17. A prepreg, characterized in that, it comprises a reinforcing material and the halogen-free resin composition of any
one of claims 1-16 which is attached on the reinforcing material after impregnation
and drying.
18. A laminate, characterized in that, it comprises at least one sheet of the prepreg of claim 17.